
Prelude Offline Takes Research Beyond the Connection
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In the realm of research, data collection is foundational. However, traditional paper-based methods and challenges with electronic data collection in…

UAT Roadmap: Quality by Design
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Part 1 – What Is Quality by Design & How to Implement It Ensuring data quality and reliable outcomes is…

Making the Switch: Reviewing Data In an EDC
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Part 5 – How to Review Data Within an Electronic Data Capture Welcome to Part 5 of our series, “Making…

Making the Switch: Building In an EDC
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Part 4 – How to Build a Study Within an Electronic Data Capture (EDC) System Welcome to Part 4 of…

Supporting GLP Compliance With Prelude EDC
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Good Laboratory Practice (GLP) is a set of principles and guidelines followed by researchers involved in non-clinical health and environmental…

Making the Switch: Writing a Protocol
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Part 3 – How to Write a Protocol to Encompass an Electronic Data Capture (EDC) System Welcome to Part 3…

Making the Switch: Validating Your EDC
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Part 2 – How to Validate Your EDC (Electronic Data Capture) System If you’re transitioning from paper to an Electronic…

Sign on the Dotted Line: Simplify the Process with eConsent
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Prelude Modules: eConsent In clinical research, obtaining informed consent from study participants is a critical component of the enrollment process. Informed…

Making the Switch: Selecting the Best EDC
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Part 1 – How to Select the Best EDC for Your Clinical Trial Needs? Looking for the right EDC for…

Doc Juggling Made Easy: Keep Studies on Track
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Prelude Modules: Document Management Document management within a study can be complicated and tedious. We know! With so many sites,…

Collecting Data for Pharmacokinetics Studies
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Prelude Modules: Pharmacokinetics (PK) When running pharmacokinetics “PK” studies, efficiency and speed are essential in getting sample data recorded….

Seamlessly Integrate IDEXX US Lab Results
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Prelude Integrations: IDEXX Labs Studies run on data. Lab result data are often key pieces of information you don’t want…

How to Design an Auditor Friendly Clinical Study
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Knock, Knock! The BIMO (or FDA QSR) auditor is at the door. It’s time to race around, retrieve documents from…

New EDC Feature for POC and Phase 1 studies
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Prelude announces a new EDC feature that streamlines data entry for Proof of Concept (POC) or Phase 1 studies. Multiple…

How NOT to Design eCRFs
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There are so many ways to design electronic CRFs. Perhaps by looking at how NOT to design them, we can…